60123017 1 2 3 4 5 104 8 8 6 1 4 -1 1 2 2 3 4 4 5 4 6 1 1 2 1 5 255 1 2 3 4 5 2 3.732 2.866 2.866 4.269 0.75 0.75 -0.75 0.25 0.44 -1 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.6.11 Cactvs xemistry.com 2019.01.04 13.5 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.6.11 Cactvs xemistry.com 2019.01.04 3 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.6.11 Cactvs xemistry.com 2019.01.04 1 Count Rotatable Bond 5 E_NROTBONDS 3.4.6.11 Cactvs xemistry.com 2019.01.04 0 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.6.11 Cactvs xemistry.com 2019.01.04 00000371000030000000000000000000000000000000000000000000000000000000000000000002000008000000000000000008000002000800000008000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.6.6 LexiChem openeye.com 2019.04.19 hydroxymethanone;rutherfordium IUPAC Name CAS-like Style 1 2.6.6 LexiChem openeye.com 2019.04.19 hydroxymethanone;rutherfordium IUPAC Name Markup 1 2.6.6 LexiChem openeye.com 2019.04.19 hydroxymethanone;rutherfordium IUPAC Name Preferred 1 2.6.6 LexiChem openeye.com 2019.04.19 hydroxymethanone;rutherfordium IUPAC Name Systematic 1 2.6.6 LexiChem openeye.com 2019.04.19 oxidanylmethanone;rutherfordium IUPAC Name Traditional 1 2.6.6 LexiChem openeye.com 2019.04.19 hydroxymethanone;rutherfordium InChI Standard 1 1.0.5 InChI iupac.org 2019.01.04 InChI=1S/CHO2.Rf/c2-1-3;/h(H,2,3);/q-1; InChIKey Standard 1 1.0.5 InChI iupac.org 2019.01.04 VDJKMRUILCLIGK-UHFFFAOYSA-N Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 312.119 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2019.01.04 CHO2Rf- Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 312.139 SMILES Canonical 1 2.1.5 OEChem openeye.com 2019.01.04 [C-](=O)O.[Rf] SMILES Isomeric 1 2.1.5 OEChem openeye.com 2019.01.04 [C-](=O)O.[Rf] Topological Polar Surface Area 7 E_TPSA 3.4.6.11 Cactvs xemistry.com 2019.01.04 37.3 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 312.119 4 0 0 0 0 0 0 0 2 -1